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1975 1
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1993 4
1995 2
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47 results

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Quoted phrase not found in phrase index: "Childhood Undifferentiated Pleomorphic Sarcoma"
Page 1
Malignant bone tumors.
Weber K, Damron TA, Frassica FJ, Sim FH. Weber K, et al. Instr Course Lect. 2008;57:673-88. Instr Course Lect. 2008. PMID: 18399615 Review.
The rarity of the condition makes it imperative that orthopaedic surgeons in nononcologic practices are able to recognize the symptoms that suggest a possible bony malignancy to avoid inappropriate or delayed treatment. The most common primary malignant bone tumors, osteos …
The rarity of the condition makes it imperative that orthopaedic surgeons in nononcologic practices are able to recognize the symptoms that …
Primary histiocytic dermatoses.
Ringel E, Moschella S. Ringel E, et al. Arch Dermatol. 1985 Dec;121(12):1531-41. Arch Dermatol. 1985. PMID: 2998286 Review.
The malignant histiocytosis with erythrophagocytosis, the pseudomalignant histiocytic diseases (such as sinus histiocytosis with massive lymphadenopathy and regressing atypical histiocytosis), and the solitary lesions with histologic malignant and atypical storiform …
The malignant histiocytosis with erythrophagocytosis, the pseudomalignant histiocytic diseases (such as sinus histiocytosis with mass …
Etiopathogenic role of ERK5 signaling in sarcoma: prognostic and therapeutic implications.
Sánchez-Fdez A, Matilla-Almazán S, Del Carmen S, Abad M, Arconada-Luque E, Jiménez-Suárez J, Chinchilla-Tábora LM, Ruíz-Hidalgo MJ, Sánchez-Prieto R, Pandiella A, Esparís-Ogando A. Sánchez-Fdez A, et al. Exp Mol Med. 2023 Jun;55(6):1247-1257. doi: 10.1038/s12276-023-01008-x. Epub 2023 Jun 19. Exp Mol Med. 2023. PMID: 37332046 Free PMC article.
By developing a mouse model engineered to express a constitutively active form of MEK5, we demonstrate that the exclusive activation of the MEK5/ERK5 pathway can promote sarcomagenesis. Histopathological analyses identified these tumors as undifferentiated pleomorphic …
By developing a mouse model engineered to express a constitutively active form of MEK5, we demonstrate that the exclusive activation of the …
Defining an embryonal rhabdomyosarcoma endotype.
Ricker CA, Crawford K, Matlock K, Lathara M, Seguin B, Rudzinski ER, Berlow NE, Keller C. Ricker CA, et al. Cold Spring Harb Mol Case Stud. 2020 Apr 1;6(2):a005066. doi: 10.1101/mcs.a005066. Print 2020 Apr. Cold Spring Harb Mol Case Stud. 2020. PMID: 32238403 Free PMC article.
Rhabdomyosarcoma (RMS) is the most common childhood soft-tissue sarcoma. The largest subtype of RMS is embryonal rhabdomyosarcoma (ERMS) and accounts for 53% of all RMS. ...Additionally, we use an unsupervised agglomerative clustering analysis of RNA and whole-exome …
Rhabdomyosarcoma (RMS) is the most common childhood soft-tissue sarcoma. The largest subtype of RMS is embryonal rhabdomyosarc …
The value of adjuvant chemotherapy in the management of sarcomas in children.
Donaldson SS. Donaldson SS. Cancer. 1985 May 1;55(9 Suppl):2184-97. doi: 10.1002/1097-0142(19850501)55:9+<2184::aid-cncr2820551422>3.0.co;2-n. Cancer. 1985. PMID: 3884137 Review.
Sarcomas of childhood rank fifth in incidence of malignant tumors in children younger than 15 years. ...The remainder represent a heterogeneous group of diverse sarcomas which are not unique to children and include fibrosarcoma, synoviosarcoma, malignant f …
Sarcomas of childhood rank fifth in incidence of malignant tumors in children younger than 15 years. ...The remainder represen …
The role of radiology in paediatric soft tissue sarcomas.
Park K, van Rijn R, McHugh K. Park K, et al. Cancer Imaging. 2008 Apr 22;8(1):102-15. doi: 10.1102/1470-7330.2008.0014. Cancer Imaging. 2008. PMID: 18442956 Free PMC article. Review.
Paediatric soft tissue sarcomas (STS) are a group of malignant tumours that originate from primitive mesenchymal tissue and account for 7% of all childhood tumours. Rhabdomyosarcomas (RMS) and undifferentiated sarcomas account for approximately 50% of soft ti …
Paediatric soft tissue sarcomas (STS) are a group of malignant tumours that originate from primitive mesenchymal tissue and account f …
New entities, concepts, and questions in childhood tumor pathology.
Harms D. Harms D. Gen Diagn Pathol. 1995 May;141(1):1-14. Gen Diagn Pathol. 1995. PMID: 8542501 Review.
A large number of new entities, especially in soft tissue tumors, have been published over the past years, including nodular mesothelial hyperplasia, which is a tumor-like lesion derived from peritoneal macrophages; infantile myofibromatosis, which can mimic leiomyosarcoma; inter …
A large number of new entities, especially in soft tissue tumors, have been published over the past years, including nodular mesothelial hyp …
Rhabdomyosarcoma in childhood.
Bale PM, Reye RD. Bale PM, et al. Pathology. 1975 Apr;7(2):101-11. doi: 10.3109/00313027509092704. Pathology. 1975. PMID: 1153222
Rhabdomyosarcomas of the female genital tract occurred only in children under 2 years, and those in the lower eyelid presented in the first year of life. A leiomyosarcoma-like appearance, and an undifferentiated small cell sarcoma sometimes mimicking Ewing's tumour, …
Rhabdomyosarcomas of the female genital tract occurred only in children under 2 years, and those in the lower eyelid presented in the first …
Soft tissue sarcomas of childhood: the differential diagnostic dilemma of the small blue cell.
Dehner LP. Dehner LP. Natl Cancer Inst Monogr. 1981 Apr;(56):43-59. Natl Cancer Inst Monogr. 1981. PMID: 6272117 Review.
The recently described small cell tumor of thoracopulmonary origin is likely a malignant neuroepithelial neoplasm. Hematopoietic tumors, such as non-Hodgkin's malignant lymphomas, granulocytic sarcoma, and malignant histiocytosis, may appear in the sof …
The recently described small cell tumor of thoracopulmonary origin is likely a malignant neuroepithelial neoplasm. Hematopoietic tumo …
Neurofibromatosis type 1 and malignancy in childhood.
Varan A, Şen H, Aydın B, Yalçın B, Kutluk T, Akyüz C. Varan A, et al. Clin Genet. 2016 Mar;89(3):341-5. doi: 10.1111/cge.12625. Epub 2015 Jul 14. Clin Genet. 2016. PMID: 26073032
Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary neurocutaneous syndrome characterized by multi-system involvement and an increased incidence of both benign and malignant tumors. In this study, we evaluated the clinical presentation and prognosis of NF1 a …
Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary neurocutaneous syndrome characterized by multi-system involvement and an …
47 results